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Color vision versus pattern visual evoked potentials in the assessment of subclinical optic pathway involvement in multiple sclerosis

BACKGROUND: Optic pathway involvement in multiple sclerosis is frequently the initial sign in the disease process. In most clinical applications, pattern visual evoked potential (PVEP) is used in the assessment of optic pathway involvement. OBJECTIVE: To question the value of PVEP against color visi...

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Autores principales: Gundogan, Fatih C, Tas, Ahmet, Altun, Salih, Oz, Oguzhan, Erdem, Uzeyir, Sobaci, Gungor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3665036/
https://www.ncbi.nlm.nih.gov/pubmed/23514643
http://dx.doi.org/10.4103/0301-4738.99842
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author Gundogan, Fatih C
Tas, Ahmet
Altun, Salih
Oz, Oguzhan
Erdem, Uzeyir
Sobaci, Gungor
author_facet Gundogan, Fatih C
Tas, Ahmet
Altun, Salih
Oz, Oguzhan
Erdem, Uzeyir
Sobaci, Gungor
author_sort Gundogan, Fatih C
collection PubMed
description BACKGROUND: Optic pathway involvement in multiple sclerosis is frequently the initial sign in the disease process. In most clinical applications, pattern visual evoked potential (PVEP) is used in the assessment of optic pathway involvement. OBJECTIVE: To question the value of PVEP against color vision assessment in the diagnosis of subclinical optic pathway involvement. MATERIALS AND METHODS: This prospective, cross-sectional study included 20 multiple sclerosis patients without a history of optic neuritis, and 20 healthy control subjects. Farnsworth-Munsell (FM) 100-Hue testing and PVEPs to 60-min arc and 15-min arc checks by using Roland-Consult RetiScan(®) system were performed. P(100) amplitude, P(100) latency in PVEP and total error scores (TES) in FM 100-Hue test were assessed. RESULTS: Expanded Disability Status Scale score and the time from diagnosis were 2.21 ± 2.53 (ranging from 0 to 7) and 4.1 ± 4.4 years. MS group showed significantly delayed P(100) latency for both checks (P < 0.001). Similarly, MS patients had significantly increased total error scores (TES) in FM-100 Hue (P < 0.001). The correlations between TESs and PVEP amplitudes / latencies were insignificant for both checks (P > 0.05 for all). 14 MS patients (70%) had an increased TESs in FM-100 Hue, 11 (55%) MS patients had delayed P(100) latency and 9 (45%) had reduced P(100) amplitude. The areas under the ROC curves were 0.944 for FM-100 Hue test, 0.753 for P(100) latency, and 0.173 for P(100) amplitude. CONCLUSIONS: Color vision testing seems to be more sensitive than PVEP in detecting subclinical visual pathway involvement in MS.
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spelling pubmed-36650362013-05-30 Color vision versus pattern visual evoked potentials in the assessment of subclinical optic pathway involvement in multiple sclerosis Gundogan, Fatih C Tas, Ahmet Altun, Salih Oz, Oguzhan Erdem, Uzeyir Sobaci, Gungor Indian J Ophthalmol Original Article BACKGROUND: Optic pathway involvement in multiple sclerosis is frequently the initial sign in the disease process. In most clinical applications, pattern visual evoked potential (PVEP) is used in the assessment of optic pathway involvement. OBJECTIVE: To question the value of PVEP against color vision assessment in the diagnosis of subclinical optic pathway involvement. MATERIALS AND METHODS: This prospective, cross-sectional study included 20 multiple sclerosis patients without a history of optic neuritis, and 20 healthy control subjects. Farnsworth-Munsell (FM) 100-Hue testing and PVEPs to 60-min arc and 15-min arc checks by using Roland-Consult RetiScan(®) system were performed. P(100) amplitude, P(100) latency in PVEP and total error scores (TES) in FM 100-Hue test were assessed. RESULTS: Expanded Disability Status Scale score and the time from diagnosis were 2.21 ± 2.53 (ranging from 0 to 7) and 4.1 ± 4.4 years. MS group showed significantly delayed P(100) latency for both checks (P < 0.001). Similarly, MS patients had significantly increased total error scores (TES) in FM-100 Hue (P < 0.001). The correlations between TESs and PVEP amplitudes / latencies were insignificant for both checks (P > 0.05 for all). 14 MS patients (70%) had an increased TESs in FM-100 Hue, 11 (55%) MS patients had delayed P(100) latency and 9 (45%) had reduced P(100) amplitude. The areas under the ROC curves were 0.944 for FM-100 Hue test, 0.753 for P(100) latency, and 0.173 for P(100) amplitude. CONCLUSIONS: Color vision testing seems to be more sensitive than PVEP in detecting subclinical visual pathway involvement in MS. Medknow Publications & Media Pvt Ltd 2013-03 /pmc/articles/PMC3665036/ /pubmed/23514643 http://dx.doi.org/10.4103/0301-4738.99842 Text en Copyright: © Indian Journal of Ophthalmology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Gundogan, Fatih C
Tas, Ahmet
Altun, Salih
Oz, Oguzhan
Erdem, Uzeyir
Sobaci, Gungor
Color vision versus pattern visual evoked potentials in the assessment of subclinical optic pathway involvement in multiple sclerosis
title Color vision versus pattern visual evoked potentials in the assessment of subclinical optic pathway involvement in multiple sclerosis
title_full Color vision versus pattern visual evoked potentials in the assessment of subclinical optic pathway involvement in multiple sclerosis
title_fullStr Color vision versus pattern visual evoked potentials in the assessment of subclinical optic pathway involvement in multiple sclerosis
title_full_unstemmed Color vision versus pattern visual evoked potentials in the assessment of subclinical optic pathway involvement in multiple sclerosis
title_short Color vision versus pattern visual evoked potentials in the assessment of subclinical optic pathway involvement in multiple sclerosis
title_sort color vision versus pattern visual evoked potentials in the assessment of subclinical optic pathway involvement in multiple sclerosis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3665036/
https://www.ncbi.nlm.nih.gov/pubmed/23514643
http://dx.doi.org/10.4103/0301-4738.99842
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